HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470801Generated: October 31, 2026
Ammonium Chloride → HCID 44201235, compound
https://huagongshe.com/reaction/470801
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 67006478 | HCID 67006478 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 44201235 | HCID 44201235 | 90.6% |
Reaction Steps
4-((1R,2S)-2-(tert-butyldimethylsilyloxy)-1-(5-(3-(tert-butyl dimethylsilyloxy)-4-fluorophenyl)-1,3,4-oxadiazol-2-yl)propylamino)-2-chloro-3-methylbenzonitrile (400 mg, 0.63 mmol) was dissolved in THF (10 mL) and cooled to −55° C. under N2 atmosphere. TBAF (1.0M solution in THF, 1.52 mL, 1.52 mmol) was added to the pre-cooled solution slowly and the temperature allowed to rise gradually. After the reaction was complete, sat. NH4Cl (200 mL) was added and the mixture was extracted with EtOAc (3×100 mL). Purification by flash chromatography over silica gel provided the desired product (230 mg). Mp 103-108° C., 1H NMR (500 MHz, acetone-d6, δ in ppm): 7.64 (d, J=9 Hz, 1H), 7.49 (m, 1H), 7.30 (t, J=9 Hz, 1H), 6.86 (d, J=9 Hz, 1H), 5.69 (d, J=9 Hz, 1H), 5.09 (m, 1H), 4.60 (m, 1H), 2.40 (s, 3H), 1.40 (d, J=6 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08629167B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-cb3608be428648138be06a390e23b0de |
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| Source note | uspto-grants-2014_01 |
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